Ccr7 aptamers and uses thereof

ABSTRACT

Disclosed herein are CCR7 aptamers that specifically bind to and internalize into CCR7-expressing cells. The aptamers can be used as a therapeutic agent by itself or in combination with a small molecule by forming a conjugate with the small molecule. Targeted delivery of the small molecule can be achieved by such conjugates. Also disclosed are methods of treating a subject suffering from cancer by administering an effective amount of the aptamer or the aptamer-small molecule conjugate to the subject.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a continuation of U.S. patent application Ser. No. 16/240,492, filed Jan. 4, 2019, which claims the benefit of U.S. provisional Patent Application No. 62/614,445, filed Jan. 7, 2018, both of which are incorporated herein by reference in their entirety, including drawings.

STATEMENT REGARDING FEDERALLY SPONSORED RESEARCH

The invention was made with government support under Grant Nos. R01 Al029329-24A1 and R01 Al042552 awarded by the National Institutes of Health (NIH), and Grant No. P30 CA033572 awarded by the National Cancer Institute (NCI) of the NIH. The government has certain rights in the invention.

SEQUENCE LISTING

This application contains a Sequence Listing, which is submitted in ASCII format via EFS Web, and is hereby incorporated by reference in its entirety. The ASCII copy, created on May 12, 2021, is named 8180US02_SequenceListing.txt and is 2 KB in size.

BACKGROUND

It has been challenging to develop aptamer-based therapeutics due to nuclease degradation. The half-life of an unmodified nucleic acid is very short, less than 10 minutes. Therefore, a need exists to develop targeted therapy as an effective and safe treatment for various diseases and conditions such as cancer. This disclosure satisfies the need in the art.

SUMMARY

The invention described herein relates to high-affinity CCR7 aptamers. In some embodiments, the aptamer is a nucleic acid aptamer, such as an RNA aptamer. In some embodiments, the aptamer is used as a therapeutic agent targeting cancer cells expressing CCR7. In other embodiments, the aptamer is used as a delivery vehicle by conjugating to a small molecule such that the small molecule is specifically delivered to the desired cell type expressing CCR7. In some embodiments, the small molecule is non-covalently conjugated to the CCR7 aptamer. In some embodiments, the small molecule includes saRNA, siRNA, shRNA or other microRNAs, a toxin, a chemotherapeutic agent, or another aptamer. In some embodiments, the aptamer is conjugated to a small molecule via one or more linkers, and/or a sticky-bridge comprising a complementary sequence. The linker can be a nucleotide linker or a polycarbon linker. In some embodiments, the aptamer, whether used as a therapeutic agent alone or used as a delivery vehicle by conjugation to a small molecule, may be chemically modified such that the half-life, stability, and/or binding affinity of the aptamer are improved.

In some embodiments, the CCR7 aptamer disclosed herein can be conjugated to one or more aptamers, such as a PD-1 aptamer, a PD-L1 aptamer, and a CD8 aptamer to generate a bi-specific aptamer conjugate, a multi-specific aptamer conjugate, or MATE.

In another aspect, methods for treating a cancer patient are provided. Such methods include administering a therapeutically effective amount of a therapeutic composition, the therapeutic composition comprising an aptamer that specifically binds to CCR7, a CCR7 aptamer conjugated to a small molecule, a bi-specific aptamer, a multi-specific aptamer, or MATE as described herein.

BRIEF DESCRIPTION OF THE DRAWINGS

This application contains at least one drawing executed in color. Copies of this application with color drawing(s) will be provided by the Office upon request and payment of the necessary fees.

FIG. 1 illustrates CCR7′s central roles in tumor cell dissemination, migration and metastasis formation. CCL21 promotes migration and invasion of cancer cells via CCR7.

FIG. 2 illustrates M-fold of examples of CCR7 aptamers.

FIG. 3 illustrates examples of CCR7 aptamer-small molecule conjugates using different linkers. Examples of small molecules include HDAC3 siRNA and CCR7 aptamer-C/EBPα saRNA.

FIG. 4 illustrates that CCR7 aptamers can be used as antagonists/delivery agents in a bi-specific aptamer system-induced T-cells to attack cancer cells and prevent T-cells deactivation.

FIG. 5 illustrates that CCR7 aptamers can be used as antagonists to generate bi-specific aptamers to increase targeting efficiency.

FIG. 6 illustrates an example of MATE, including a CCR7 aptamer, which identifies CCR7 expressing cancer cells; a PD-1 aptamer, which blocks PD-1/PD-L1 signaling and identifies CD8+ T cells; and a CD8 aptamer, which identifies CD8⁺ T cells.

FIG. 7 illustrates targeting cancer by CCR7-MATE. ON: active CD8⁺ T cells; TCR: T cell receptor; MHC: major histocompatibility complex.

FIG. 8 illustrates binding affinity (Kd) of additional examples of CCR7 aptamers such as C-1A and C-2A (SEQ ID NOS:1-3).

FIG. 9 shows internalization of CCR7 aptamers into CCR7-expressing cells.

FIG. 10 shows that CCR7 aptamer-siRNA conjugates mediated specific gene silencing in CCR7-expressing H9 cells, while non-CCR7-conjugated siRNA had no silencing effect in the assay.

FIG. 11 shows that CCR7 aptamer-saRNA conjugate mediated specific gene activation in CCR7-expressing H9 cells, while other constructs did not.

FIG. 12 shows that CCR7 aptamer-C/EBPa saRNA conjugate inhibited cell proliferation in CCR7-expressing H9 cells but not in Jurkat cells.

DETAILED DESCRIPTION

Cell type-specific aptamers that selectively bind human CCR7 protein, systems for cell type-specific delivery of small molecules and methods for their use are provided herein. According to the embodiments described herein, the cell type-specific aptamers can be used as effective RNA-based targeted cancer therapies. In addition to their utility as stand-alone therapeutics, cell type-specific aptamers can also serve as a new therapeutic modality by functioning as a delivery vehicle for another therapeutic. Thus, cell-type specific aptamer-based nano-conjugates for targeted cancer therapy are also disclosed herein.

Cell Type-Specific Aptamers

Aptamers^(1,2), often termed “chemical antibodies,” are short, single-stranded (ss) DNA or RNA molecules that bind to a specific target. They are typically selected through systematic enrichment of ligands by exponential enrichment (SELEX) technology³. Aptamers are functionally comparable to antibodies, but possess many additional attractive features, including relatively small physical size (nano-scale), flexible structure, quick chemical production, versatile chemical modification, high stability, and lack of immunogenicity. As such, they show increasing potential for therapeutic applications^(4,5). Aptamers can serve as direct antagonists for blocking the interaction of disease-associated targets, or as target-specific carriers for delivering other therapeutic agents (e.g. siRNA, shRNA, microRNA, other aptamers, chemotherapeutics, or toxins)⁶.

Human CC chemokine receptor 7 (CCR7), a member of the G protein-coupled receptor family, is known to control migration of memory T-cells to inflamed organs, such as lymph node. CCR7 is expressed by various cancer cells, such as breast cancer, melanoma, non-small cell lung cancer, prostate cancer, chronic lymphocytic leukemia (CLL), non-Hodgkin's lymphoma (NHL), T-cell leukemia, etc. Expression of CCR7 by cancer cells is linked to metastasis to lymph node. The signal transduction pathways triggered by CCR7 engagement through its ligands, the chemokines CCL19 and CCL21, represent a promising target for cancer therapy. Thus, CCR7 is a convenient target for aptamers and their conjugates. FIG. 1 illustrates CCR7′s central roles in tumor cell dissemination, migration and metastasis formation.

Disclosed herein are high-affinity CCR7 aptamers that are capable of selectively binding to CCR7-expressing cells and being internalized specifically into CCR7-expressing cells, as well as methods and assays for screening and identifying such aptamers having high affinity for CCR7. The therapeutic aptamers disclosed herein, either used alone or in combination with small molecules, can specifically target CCR7-expressing cancer cells and improve tumor suppression.

In one embodiment, aptamers for targeting certain cell types, such as CCR7-expressing tumor cells, are provided as a cancer therapy for breast cancer, melanoma, non-small cell lung cancer, prostate cancer, chronic lymphocytic leukemia (CLL), non-Hodgkin's lymphoma (NHL), T-cell leukemia, etc. An “aptamer” is any suitable small molecule, such as a nucleic acid or a peptide molecule that binds specifically to a target, such as a small molecule, protein, nucleic acid, cell, tissue or organism. Aptamers that target specific cell surface proteins can be employed as delivery molecules to target a distinct cell type, thereby reducing off-target effects or other unwanted side effects. Further, by binding a specific cell surface protein, the aptamers may also be used as therapeutic agents on their own.

In some embodiments, the therapeutic effects of the disclosed aptamers can be improved by developing bivalent aptamer conjugates to achieve higher avidity to the target. In certain embodiments, conjugation can be optimized by varying the length and/or sequence of the linker or sticky bridge such that the correct structure of the selected aptamers and the activity of therapeutic agents can be maximally retained. In some embodiments, the linker, e.g., a polycarbon linker, has a length of between 3 units and 10 units, each unit having 3 carbons. In some embodiments, the sticky bridge has a GC-rich sequence. In some embodiments, the sticky bridge has a length of between 5 bp and 30 bp. In some embodiments, the sticky bridge has a length of 5 bp, 6 bp, 7, bp, 8 bp, 9 bp, 10 bp, 11 bp, 12 bp, 13 bp, 14 bp, 15 bp, 16 bp, 17 bp, 18 bp, 19 bp, 20 bp, 21 bp, 22 bp, 23 bp, 24 bp, 25 bp, 26 bp, 27 bp, 28 bp, 29 bp, or 30 bp. Additionally, two nano-conjugates can be combined to further improve the targeting and therapeutic effects. For example, combinational use of various RNA therapeutics can achieve synergistic effects.

Therefore, in some embodiments, a cell-type specific aptamer that targets and binds CCR7 is provided. In one embodiment, the aptamer is a nucleic acid molecule. For example, the nucleic acid CCR7 aptamer can be an RNA aptamer molecule. FIG. 2 shows M-fold of some examples of the aptamers disclosed herein.

The CCR7 aptamers share the same 5′ and 3′ fixed regions. The core sequences (underlined) of these aptamers are different.

C-1A aptamer: (SEQ ID NO: 1) 5′-GGGAGGACGAUGCGGUUUCGUCCUGAGUUCGUGUCCUCGUCUGUGCAG ACGACUCGCCCGA-3′ C-2A aptamer: (SEQ ID NO: 2) 5′-GGGAGGACGAUGCGGAAUUCGUCAAAGUCGUUUAUUUCGUCUGUGCAG ACGACUCGCCCGA-3′ DD9-9 aptamer: (SEQ ID NO: 3) 5′-GGGAGGACGAUGCGGUGCCGCACAUUAGUCUCUGGUUGCCCACGCCAG ACGACUCGCCCGA-3′ C-6 aptamer: (SEQ ID NO: 4) 5′-GGGAGGACGAUGCGGUCCAUCGUCUCUUAUCGUCUCUUGUCGCGCCAG ACGACUCGCCCGA-3′

Nucleic acid aptamers with binding affinities in nanomolar range have been utilized for flexible applications ranging from diagnostic to therapeutic assay formats. Moreover, aptamers that target CCR7 are employed as delivery molecules to target a distinct cell type, e.g., tumor cells, hence reducing off-target effects or other unwanted side effects.

Selection and characterization of CCR7 RNA aptamers

In some embodiments, disclosed herein are methods of identifying RNA aptamers directed to human CCR7. The method includes synthesizing representative aptamers for further characterization and determining their binding affinity, target specificity, and ability to be internalized within cells expressing CCR7. The method further includes assessing which CCR7 aptamers functionally antagonize CCR7 activities.

Selection of aptamers may be accomplished by an optimized protocol for in vitro selection, known as SELEX (Systemic Evolution of Ligands by Exponential enrichment). Although the SELEX process has been established as a general technique for aptamer selection, it is not predictable nor is it standardized for use with any target. Instead, the SELEX process must be optimized and customized for each particular target molecule. Each SELEX experiment includes its own challenges and is not guaranteed to work for all targets.

Many factors are important for successful aptamer selection. For example, the target molecule should be stable and easily reproduced for each round of SELEX, because the SELEX process involves multiple rounds of binding, selection, and amplification to enrich the nucleic acid molecules. In addition, the nucleic acids that exhibit specific binding to the target molecule have to be present in the initial library. Thus, it is advantageous to produce a highly diverse nucleic acid pool. Because the starting library is not guaranteed to contain aptamers to the target molecule, the SELEX process for a single target may need to be repeated with different starting libraries. Aptamer selection using SELEX is unpredictable. Even when all of the factors are optimized for successful aptamer selection, the SELEX process does not always yield viable aptamers for every target molecule.

As described herein, a well-established “Live cell-based SELEX” strategy⁷ is combined with high throughput sequencing (HTS) technology and bioinformatics analysis to identify new 2′-fluoropyrimidine modified CCR7 RNA aptamers that are capable of specifically targeting the CCR7-expressing cells. HeLa cells that stably over-express CCR7 can be used. Selected CCR7 aptamers bind specifically and are internalized into the CCR7-expressing HeLa cells. In some embodiments, seven selection rounds containing both positive and negative selection are performed with cell-specific binding and internalization of the RNA libraries. Barcode-based Illumina deep sequencing technology can be used to identify the individual aptamer sequences for the RNA pools from selection rounds 0-7. During SELEX procedures, a specific enrichment was observed.

Modification of Aptamers

To increase the half-life, stability and/or binding affinity of aptamers, particularly nucleic acid aptamers, the selected aptamers are chemically modified, for example, by replacing the 2′ position with either a fluoro-(F), amino-(NH₂), or O-methyl (OCH₃) group, and by capping the 3′ end with inverted thymidine to increase nuclease resistance while also enhancing binding affinity. The aptamers can be modified in-SELEX and/or post-SELEX.

For in-SELEX modifications, aptamers with the desired modifications are directly isolated from a DNA or RNA library containing modified nucleotides that are compatible with DNA or RNA polymerases. The aptamers that can be modified by this method include 2′-aminopyrimidines, 2′-fluoropyrimidines, 2′-O-methyl nucleotides and locked nucleic acids (LNA).

As for post-SELEX modifications, different modifications at various positions (e.g., base, 2′-position, sugar ring, phosphate group) can be introduced to selected aptamers during solid-phase chemical synthesis. Since the affinity/specificity and function of an aptamer depend on its structure, post-SELEX modification may affect the inherent properties and folding structures of the original aptamers, thereby compromising the binding affinity. Therefore, it is necessary to precisely tailor modifications to optimize the desired functions.

Various chemical modifications to stabilize aptamers are disclosed in the art, for example, Gijs M., et al., Nuclear Medicine and Biology, 43(4): 253-271 (2016); and Yu Y, et al. International Journal of Molecular Sciences, 17(3): 358 (2016).

Cell Type-Specific Aaptamer-Based Nano-Conjugates

Disclosed are cell type-specific aptamer-based small RNA nano-conjugates for targeted cancer therapy. These cell type-specific CCR7 aptamers bind and selectively enter into the cells expression CCR7. Various small RNAs, e.g., siRNAs and saRNAs, can be conjugated to the CCR7 aptamer, and these conjugates can be used to accommodate target genetic changes. Thus, these cell-specific, internalizing RNA aptamers can be used for cell type-specific gene silencing or activation for targeted treatment of CCR7-expressing cancers.

Engineering various aptamer-based nano-conjugates using a non-covalent conjugation approach is disclosed herein. In some embodiments, cell-type-specific aptamer-based nano-conjugates can be used to deliver small molecules such as functional nucleic acids into CCR7-expressing tumor cells. Some examples of the nano-conjugates include but are not limited to aptamer-small activating RNA (saRNA) conjugates, and aptamer-siRNA conjugates. The nano-conjugates disclosed herein are efficacious in suppressing tumors growth through specifically targeting to CCR7 expressing cancer cells. The effect of the aptamer-based nano-conjugates is determined based on the specificity of delivery, targeted gene regulation, and inhibition of tumor cell proliferation.

In some embodiments, a selected aptamer can be linked to a small molecule through a complementary “sticky sequence” or “sticky bridge” to generate an aptamer-small molecule conjugate.

To determine which conjugates specifically bind and are internalized into target cells, flow cytometry and live-cell confocal microscopy experiments can be performed as described above. The binding affinity test is performed using cell lines expressing target protein as well as primary cells.

Thus, in addition to their utility as stand-alone therapeutics, aptamers disclosed herein can be used as escorts for another therapeutics by forming a conjugate of a cell type-specific aptamer and a small molecule therapeutic agent. Such small molecule therapeutic agents include but are not limited to, for example, saRNA, siRNA, shRNA, microRNA, anti-miR, a therapeutic aptamer, a chemotherapeutic, a toxin, a radioisotope, an antisense oligonucleotides, a photoactive agent, and a dye.

The small molecule that is conjugated to the aptamers disclosed herein may include any suitable short RNA structure including, but not limited to, siRNAs, shRNAs, miRNAs and other short dsRNAs. In one embodiment, the siRNA molecule may be a traditional monofunctional siRNA molecule having a functional antisense strand and a complementary sense strand. In some embodiments, known anti-cancer siRNA molecules, such as siRNAs targeting histone deacetylase 3 (HDAC3) or CCAAT/enhancer-binding protein-α (C/EBPα) can be used.

HDAC3 (histone deacetylase 3) is essential for efficient DNA replication and DNA damage control, which was found to be highly expressed in various tumors, such as renal cell cancer, colorectal and gastric cancer as well as in classical Hodgkin's lymphoma. siRNA-mediated knockdown of HDAC3 in HeLa cells results in inhibition of cell proliferation.

C/EBPα (CCAAT/enhancer-binding protein-α) is a transcriptional regulator that plays an essential role in tumor metastasis. saRNA-mediated enhanced C/EBPa expression can reduce tumor burden and metastasis.

In another embodiment, the aptamer-small molecule conjugate is constructed by a method of non-covalent conjugation. Non-covalent conjugation involves chemically linking two molecules without sharing of pairs of electrons. Non-covalent conjugation may involve electrostatic interactions such as hydrogen bonds, ionic bonds, van der Waals forces and hydrophobic interactions.

Multi-Specific Aptamer Conjugates

In some embodiments, two or more aptamers can be conjugated via any of the linkers disclosed herein or via non-covalent conjugation to generate bi-specific or multi-specific aptamer conjugates. For example, the CCR7 aptamer disclosed herein can be conjugated to a PD-1 aptamer to form a bi-specific aptamer conjugate, which can induce T-cells to attack cancer cells and prevent T-cells deactivation, as illustrated in FIG. 4. In another example, the CCR7 aptamer disclosed herein can be conjugated to a PD-L1 aptamer to form a bi-specific aptamer conjugate, which can increase targeting efficiency, as illustrated in FIG. 5.

It has been demonstrated that conjugating cell-specific aptamers to therapeutic agents can facilitate specific recognition and intracellular internalization to the targeted cells, thereby improving the local concentration of the drugs and their therapeutic efficacy. A bi-specific aptamer conjugate consisting of high-affinity aptamers against c-Met and CD16a specifically recruited NK (natural killer) cells to c-Met-overexpressing tumor cells, consequently inducing tumor cell lysis. Thus, also disclosed herein are cell-specific aptamers that possess high binding affinity and exquisite specificity to engage CD8⁺ T cells to target CCR7-expressing tumor cells and induce CD8⁺ T cell-dependent killing.

In some embodiments, disclosed herein is a Multi-specific Aptamers-based T cells Engager (MATE: CD8/PD-1/CCR7) (see FIG. 6). The MATE simultaneously binds and engages CD8⁺ T cells (via CD8 and PD-1) and tumor cells (via CCR7) and drives killer T cells to eliminate CCR7-expressing tumor cells, as illustrated in FIG. 7. As shown in the figures, a MATE containing three aptamers specific to CD8, PD-1 and CCR7 functions as a bridge to engage CD8⁺ T cells (CD8⁺/PD-1⁺) and tumor cells (CCR7+) to induce special cytotoxicity.

Treatment of Cancer

The CCR7 aptamers, the aptamer-small molecule conjugates, bi-specific or multi-specific aptamer conjugates, and MATE described herein can be used for specifically targeting CCR7-expressing cells as well as a therapy for cancer. Therefore, methods for treating a subject suffering from various cancer are provided according to the embodiments described herein.

“Treating” or “treatment” of a disease or a condition may refer to preventing the disease or condition, slowing the onset or rate of development of the disease or condition, reducing the risk of developing the disease or condition, preventing or delaying the development of symptoms associated with the disease or condition, reducing or ending symptoms associated with the disease or condition, generating a complete or partial regression of the disease or condition, or some combinations thereof.

The method for treating a cancer includes administering a therapeutically effective amount of a therapeutic composition. An “effective amount,” “therapeutically effective amount” or “effective dose” is an amount of a composition (e.g., a therapeutic composition or agent) that produces a desired therapeutic effect in a subject, such as preventing or treating the cancer or alleviating symptoms associated with the cancer.

The precise therapeutically effective amount is an amount of the composition that will yield the most effective results in terms of efficacy of treatment in a given subject. This amount will vary depending upon a variety of factors, including but not limited to the characteristics of the therapeutic compound (including activity, pharmacokinetics, pharmacodynamics, and bioavailability), the physiological condition of the subject (including age, sex, disease type and stage, general physical condition, responsiveness to a given dosage, and type of medication), the nature of the pharmaceutically acceptable carrier or carriers in the formulation, and the route of administration. One skilled in the clinical and pharmacological arts will be able to determine a therapeutically effective amount through routine experimentation, namely by monitoring a subject's response to administration of a compound and adjusting the dosage accordingly. For additional guidance, see Remington: The Science and Practice of Pharmacy 21^(st) Edition, Univ. of Sciences in Philadelphia (USIP), Lippincott Williams & Wilkins, Philadelphia, Pa., 2005.

The therapeutic composition may include, among other things, an aptamer, and/or an aptamer-small molecule conjugate described herein. For example, in some embodiments, an RNA aptamer that may be part of the therapeutic composition.

The therapeutic composition may also include one or more pharmaceutically acceptable carriers. A “pharmaceutically acceptable carrier” refers to a pharmaceutically acceptable material, composition, or vehicle that is involved in carrying or transporting a compound of interest from one tissue, organ, or portion of the body to another tissue, organ, or portion of the body. For example, the carrier may be a liquid or solid filler, diluent, excipient, solvent, or encapsulating material, or some combination thereof. Each component of the carrier must be “pharmaceutically acceptable” in that it must be compatible with the other ingredients of the formulation. It also must be suitable for contact with any tissue, organ, or portion of the body that it may encounter, meaning that it must not carry a risk of toxicity, irritation, allergic response, immunogenicity, or any other complication that excessively outweighs its therapeutic benefits.

The therapeutic compositions described herein may be administered by any suitable route of administration. A route of administration may refer to any administration pathway known in the art, including but not limited to aerosol, enteral, nasal, ophthalmic, oral, parenteral, rectal, transdermal (e.g., topical cream or ointment, patch), or vaginal. “Transdermal” administration may be accomplished using a topical cream or ointment or by means of a transdermal patch. “Parenteral” refers to a route of administration that is generally associated with injection, including infraorbital, infusion, intraarterial, intracapsular, intracardiac, intradermal, intramuscular, intraperitoneal, intrapulmonary, intraspinal, intrasternal, intrathecal, intrauterine, intravenous, subarachnoid, subcapsular, subcutaneous, transmucosal, or transtracheal. In some embodiments, the therapeutic compositions described herein are administered by intravenous injection or intraperitoneal injection.

Having described the invention with reference to the embodiments and illustrative examples, those in the art may appreciate modifications to the invention as described and illustrated that do not depart from the spirit and scope of the invention as disclosed in the specification. The examples are set forth to aid in understanding the invention but are not intended to, and should not be construed to limit its scope in any way. The examples do not include detailed descriptions of conventional methods. Such methods are well known to those of ordinary skill in the art and are described in numerous publications. Further, all references cited above and in the examples below are hereby incorporated by reference in their entirety, as if fully set forth herein.

EXAMPLES Example 1 Binding and Internalization of CCR7 Aptamers

This example demonstrates that CCR7 aptamers selectively bind to CCR7-expressing cells and are internalized specifically into CCR7-expressing cells.

As shown in Table 1, CCR7 aptamers demonstrated high binding affinity to CCR7-positive HeLa cells, CCR7-positive H9 cells, and CCR7-positive human memory CD4+ T cells.

TABLE 1 Binding Affinity of CCR7 Aptamers As analyzed by flow cytometry analysis (CCR7-positive cells) As analyzed by Candidate HeLa-CCR7 H9-CCR7 Human memory gel shift assay CCR7 positive positive CD4+ T cells Recombinant aptamers cells cells (CCR7 positive) CCR7 protein C-1A +++ +++ ++ ++ C-2A +++ +++ ++ +++ C-5B + +++ + + C-6 ++ ++ + + +++: >50% binding affinity ++: 30-50% binding affinity +: 10-25% binding affinity

As shown in FIG. 8, binding affinity of CCR7 aptamers was dose-dependent and CCR7 aptamer C-1A demonstrated the highest binding affinity.

As shown in FIG. 9, CCR7 aptamers were internalized specifically into CCR7-expressing cells.

Example 2 Gene Silencing Effects of CCR7 Aptamer-Small RNA Nano-Conjugates

CCR7 aptamers, C-1A and C-2A, were conjugated to HDAC2 siRNA and HDAC3 siRNA respectively. The silencing effects of the CCR7 aptamers alone, siRNAs alone, and the CCR7 aptamer-siRNA conjugates were tested in H9 cells having a high expression level of CCR7 and Jurkat cells having a low expression level of CCR7. As demonstrated by FIG. 10, CCR7 aptamer-siRNA conjugates demonstrated specific gene silencing effects in CCR7 expressing H9 cells, while the aptamers alone and non-CCR7-conjugated siRNAs did not show silencing effects.

Example 3 Gene Activating Effects of CCR7 Aptamer-Small RNA Nano-Conjugates

CCR7 aptamer, C-1A, was conjugated to C/EBPa saRNA and an unrelated saRNA respectively. The activating effects of the CCR7 C-1A aptamer alone, saRNAs alone, and the CCR7 aptamer-saRNA conjugates were tested in H9 cells having a high expression level of CCR7 and Jurkat cells having a low expression level of CCR7. Two dose of 400 nM of experimental RNAs were directly incubated with H9 cells or Jurkat cells at day 1 and day 2. At 48 hour post-incubation, total RNA was isolated for qRT-PCR analysis. As demonstrated by FIG. 11, only the CCR7 aptamer-C/EBPα saRNA conjugate demonstrated specific gene activating effects on the target gene C/EBPα (left) and its downstream gene p21 (right) in CCR7-expressing H9 cells, while other constructs did not show activating effects. The results suggested that CCR7 aptamer-based RNA nano-conjugates selectively delivered saRNA into CCR7 expressing cells, therefore specifically upregulating the target gene as well as its downstream gene.

Example 4 Inhibition of Cell Proliferation by CCR7 Aptamer-Small RNA Nano-Conjugates

CCR7 aptamer, C-1A, was conjugated to C/EBPa saRNA, and the effects of the conjugate on cell proliferation were tested in H9 cells expressing a high level of CCR7 and in Jurkat cells expressing a low level of CCR7. Two dose of 400 nM of experimental RNAs were directly incubated with H9 cells or Jurkat cells at day 1 and day 2. At 48 hour post-incubation, MTS assay was conducted to determine the cell viability. As demonstrated by FIG. 12, the CCR7 aptamer-C/EBPα saRNA conjugate inhibited specific cell proliferation by inhibiting about 40% cell proliferation in H9 cells which expressed a high level of CCR7 but had no effect on Jurkat cells which expressed a low level of CCR7. 72 hours post-treatment showed the best suppression on cell proliferation. Collectively, it was demonstrated that CCR7 aptamer-based RNA nano-conjugates selectively delivered saRNA into CCR7 expressing cells, therefore specifically inhibiting the target cells proliferation.

REFERENCES

The references listed below, and all references cited in the specification are hereby incorporated by reference in their entireties, as if fully set forth herein.

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3 Darmostuk, M., Rimpelova, S., Gbelcova, H. & Ruml, T. Current approaches in SELEX: An update to aptamer selection technology. Biotechnol Adv 33, 1141-1161, doi:10.1016/j.biotechadv.2015.02.008 (2015).

4 Keefe, A. D., Pai, S. & Ellington, A. Aptamers as therapeutics. Nature reviews. Drug discovery 9, 537-550, doi:10.1038/nrd3141 (2010).

5 Sundaram, P., Kurniawan, H., Byrne, M. E. & Wower, J. Therapeutic RNA aptamers in clinical trials. Eur J Pharm Sci 48, 259-271, doi:S0928-0987(12)00414-9 [pii] 10.1016/j.ejps.2012.10.014 (2013).

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1. A cell-type specific aptamer-small molecule conjugate com prising: an aptamer that specifically binds CCR7, and a small molecule conjugated to the aptamer via non-covalent conjugation, wherein the CCR7 aptamer is C-1A (SEQ ID NO: 1), C-2A (SEQ ID NO: 2), DD9-9 (SEQ ID NO: 3), or C-6 (SEQ ID NO: 4).
 2. The aptamer-small molecule conjugate of claim 1, wherein the aptamer is an RNA molecule.
 3. The aptamer-small molecule conjugate of claim 1, wherein the aptamer is chemically modified in-SELEX or post-SELEX.
 4. The aptamer-small molecule conjugate of claim 1, wherein the aptamer is chemically modified by replacing the 2′ position with either a fluoro-(F), amino-(NH₂), or O-methyl (OCH₃) group, and by capping the 3′ end with inverted thymidine.
 5. The aptamer-small molecule conjugate of claim 1, wherein the small molecule is an saRNA, an siRNA, an shRNA, an miRNA, a different aptamer, a chemotherapeutic agent, or a toxin.
 6. The aptamer-small molecule conjugate of claim 5, wherein the saRNA targets CCAAT/enhancer-binding protein-α.
 7. The aptamer-small molecule conjugate of claim 1, wherein the conjugate is a bispecific aptamer-aptamer conjugate.
 8. The aptamer-small molecule conjugate of claim 7, wherein one aptamer binds CCR7 and the other aptamer binds PD-1 or PD-L1.
 9. The aptamer-small molecule conjugate of claim 1, wherein the aptamer is conjugated to the small molecule via one or more linkers.
 10. The aptamer-small molecule conjugate of claim 9, wherein the linker is a nucleotide linker or a polycarbon linker.
 11. The aptamer-small molecule conjugate of claim 1, wherein the aptamer is conjugated to the small molecule via a sticky bridge comprising a complementary sequence.
 12. A MATE comprising a CCR7 aptamer, a PD-1 aptamer, and a CD8 aptamer, wherein the CCR7 aptamer is C-1A (SEQ ID NO: 1), C-2A (SEQ ID NO: 2), DD9-9 (SEQ ID NO: 3), or C-6 (SEQ ID NO: 4).
 13. A method for treating a cancer patient comprising administering a therapeutically effective amount of a therapeutic composition, wherein the therapeutic composition comprises a CCR7 aptamer, a conjugate of a CCR7 aptamer and a small molecule, or a MATE comprising a CCR7 aptamer, a PD-1 aptamer, and a CD8 aptamer, wherein the CCR7 aptamer is C-1A (SEQ ID NO: 1), C-2A (SEQ ID NO: 2), DD9-9 (SEQ ID NO: 3), or C-6 (SEQ ID NO: 4).
 14. The method of claim 13, wherein the aptamer is an RNA molecule.
 15. The method of claim 13, wherein the aptamer is chemically modified in-SELEX or post-SELEX.
 16. The method of claim 13, wherein the aptamer is chemically modified by replacing the 2′ position with either a fluoro-(F), amino-(NH2), or 0-methyl (OCH₃) group, and by capping the 3′ end with inverted thymidine.
 17. The method of claim 13, wherein the small molecule includes an saRNA, an siRNA, an shRNA, an miRNA, a different aptamer, a chemotherapeutic agent, and a toxin.
 18. The method of claim 13, wherein the patient suffers from breast cancer, melanoma, non-small cell lung cancer, prostate cancer, chronic lymphocytic leukemia (CLL), non-Hodgkin's lymphoma (NHL), or T-cell leukemia.
 19. The aptamer-small molecule conjugate of claim 1, wherein the CCR7 aptamer is C-1A (SEQ ID NO: 1), or C-2A (SEQ ID NO: 2).
 20. The method of claim 13, wherein the CCR7 aptamer is C-1A (SEQ ID NO: 1), or C-2A (SEQ ID NO: 2). 